ClearanceBrief
510(k) K944293 ยท FPA Set, Administration, Intravascular

SABRATEK SABSIL SETS

ApplicantSabratek Corp., Niles IL, US
DecisionSubstantially Equivalent, Mar 23, 1995
ReceivedSep 2, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944293

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.